HuagongsheHuagongshe Chemistry Print Report · For research reference only
beta-Phenylisovaleric acid → 3-Methyl-3-phenylbutan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | beta-Phenylisovaleric acid | HCID 13890 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methyl-3-phenylbutan-1-ol | HCID 232460 | — |
Reaction Steps
3-Methyl-3-phenylbutanoic acid (0.90 9) was dropwise added to a suspension of lithium alminum hydride (0.2 g) in 15 ml of tetrahydrofuran at room temperature and the mixture was stirred for 30 minutes. To the reaction mixture was added a saturated aqueous solution of sodium bicarbonate under ice cooling, and the reaction solution was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride,, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resultant residue was subjected to silica gel column chromatography (20 g). Elution with a hexane ethyl acetate (5:1) mixture gave 0.75 g of 3-metyl-3-phenylbutanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04987132 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-f44441e6c92241f4803cf0b43b831589 |
| Source note | uspto-grants-1991_01 |